A drug-free nanozyme for mitigating oxidative stress and inflammatory bowel disease

促炎细胞因子 炎症性肠病 炎症 氧化应激 活性氧 免疫学 化学 医学 疾病 病理 生物化学
作者
Feng Zeng,Yahong Shi,Chunni Wu,Jianming Liang,Qixin Zhong,Karen Briley,Bin Xu,Yongzhuo Huang,Manmei Long,Cong Wang,Jian Chen,Yonghua Tang,Xinying Li,Mengda Jiang,Luting Wang,Qin Xu,Yang Liu,Peng Chen,Sheng‐Zhong Duan,Jingyuan Xie
出处
期刊:Journal of Nanobiotechnology [BioMed Central]
卷期号:20 (1) 被引量:44
标识
DOI:10.1186/s12951-022-01319-7
摘要

Inflammatory bowel disease (IBD) is an incurable disease of the gastrointestinal tract with a lack of effective therapeutic strategies. The proinflammatory microenvironment plays a significant role in both amplifying and sustaining inflammation during IBD progression. Herein, biocompatible drug-free ceria nanoparticles (CeNP-PEG) with regenerable scavenging activities against multiple reactive oxygen species (ROS) were developed. CeNP-PEG exerted therapeutic effect in dextran sulfate sodium (DSS)-induced colitis murine model, evidenced by corrected the disease activity index, restrained colon length shortening, improved intestinal permeability and restored the colonic epithelium disruption. CeNP-PEG ameliorated the proinflammatory microenvironment by persistently scavenging ROS, down-regulating the levels of multiple proinflammatory cytokines, restraining the proinflammatory profile of macrophages and Th1/Th17 response. The underlying mechanism may involve restraining the co-activation of NF-κB and JAK2/STAT3 pathways. In summary, this work demonstrates an effective strategy for IBD treatment by ameliorating the self-perpetuating proinflammatory microenvironment, which offers a new avenue in the treatment of inflammation-related diseases.
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